Evidence map›Paper›PMID 24101375›Full record

ArticleThe Journal of experimental medicine2013

Transcription factor Runx2 controls the development and migration of plasmacytoid dendritic cells.

Catherine M Sawai, Vanja Sisirak, Hiyaa S Ghosh, Esther Z Hou, Michele Ceribelli, Louis M Staudt, Boris Reizis

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

85 citing papers in PubMed, 129 citations in OpenAlex.

  1. Review
  2. Article
  3. Human Blood IgAEuropean journal of immunology · 2026
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  5. Review
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  7. Article
  8. Review
  9. Review
  10. Unexpected heterogeneity and tissue-specific properties of the thymic hematopoietic antigen-presenting cell network.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  14. C/EBPα activatesScience immunology · 2025
    Article
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  16. Article
  17. Lung Immune Cell Niches and the Discovery of New Cell Subtypes.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  18. Article
  19. Article
  20. Article

25 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Catherine M SawaiDepartment of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032.
Vanja Sisirak
Hiyaa S Ghosh
Esther Z Hou
Michele Ceribelli
Louis M Staudt
Boris Reizis
Columbia University Irving Medical Center · USNational Cancer Institute · US

Funding

Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR01AI072571 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2008 to 2017
$4.1M
NIAID NIH HHS AI072571NIAID NIH HHS R01 AI072571
6 · The paper itself

Abstract

Plasmacytoid dendritic cells (pDCs) rapidly produce type I interferon (IFN-I) in response to viruses and are essential for antiviral immune responses. Although related to classical DCs (cDCs) in their development and expression profile, pDCs possess many distinct features. Unlike cDCs, pDCs develop in the bone marrow (BM) and emerge into peripheral lymphoid organs and tissues as fully differentiated cells. We now report that pDCs specifically express Runx2, a Runt family transcription factor that is essential for bone development. pDCs in Runx2-deficient mice developed normally in the BM but were greatly reduced in the periphery. The defect was cell-intrinsic and was associated with the retention of mature Ly49Q(+) pDCs in the BM. Runx2 was required for the expression of several pDC-enriched genes, including the chemokine receptors Ccr2 and Ccr5. Mature pDCs expressed high levels of Ccr5 at the cell surface, and Ccr5-deficient pDCs in a competitive setting were reduced in the periphery relative to the BM. Thus, Runx2 is required for the emergence of mature BM pDCs into the periphery, in a process that is partially dependent on Ccr5. These results establish Runx2 as a lineage-specific regulator of immune system development.

Indexed as

Cell DifferentiationCell MovementAnimalsBone Marrow CellsCore Binding Factor Alpha 1 SubunitDendritic CellsGene DeletionGene Expression RegulationHumansMiceMice, Inbred C57BLMice, KnockoutNK Cell Lectin-Like Receptor Subfamily AReceptors, CCR5Transcription Factor 7-Like 2 ProteinTranscription FactorsCore Binding Factor Alpha 1 SubunitKlra17 protein, mouseNK Cell Lectin-Like Receptor Subfamily AReceptors, CCR5Runx2 protein, mouseTCF7L2 protein, humanTranscription Factor 7-Like 2 ProteinTranscription Factors

Identifiers

PMID24101375
PMCPMC3804932
OpenAlexW2161595265

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.